Herein, an unprecedented synthetic route to sulfilimines via a copper-catalyzed Chan–Lam-
type coupling of sulfenamides is presented. A key to success in this novel transformation is …

Sulfur‐containing functional groups have garnered considerable attention due to their
common occurrence in ligands, pharmaceuticals, and insecticides. Nevertheless …

In this research paper, aromatic sulfonamide-derived ethyl ester (p-TSAE) and its acyl
hydrazide (p-TSAH) were directly synthesized, characterized, and employed for the first time …

Accelerated SuFEx Click Chemistry (ASCC) is a powerful method for coupling aryl and alkyl
alcohols with SuFEx-compatible functional groups. With its hallmark favorable kinetics and …

Functionalized aryl sulfonamides are important building blocks in the pharmaceutical
industry. A one-step synthesis catalyzed by a copper salt was developed using stable solid …

This review disclosed synthetic approaches to sulfonyl amides from non‐sulfonyl
halogenated precursors. Known methods were systematized into groups and subgroups …

A visible‐light‐triggered synthesis of sulfonamide was developed via an electron donor‐
acceptor (EDA) complex in the more environmentally friendly green solvent 2 …

(Hetero) arylethylamines are privileged substructures in pharmaceuticals, agrochemicals,
and other bioactive compounds. In principle, the amino–(hetero) arylation of olefins …

The unique features of the sulfenamides' S (II)-N bond lead to interesting stereochemical
properties and significant industrial functions. Here we present a chemoselective Chan–Lam …

A thiosuccinimide enabled S–N cross-coupling strategy has been established for the
intermolecular N-sulfenylation of clinically approved sulfa drugs under additive-free …